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Macupatide

Phase 2

Obesity | Small molecule | Metabolic |Eli Lilly and Company|Last Updated: Jun 4, 2026

Success Probability
Approval Probability 71%
TA Base Rate26%
Adjusted LOA41%
ML RiskLOW_RISK
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Market & Valuation
rNPV $3.2B
Market Size $9.4B
Revenue Basis $1.6B
Competitors 6
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Trial Design
RandomizedDouble-BlindPLACEBO_CONTROLLEDBiomarker
Total Trials1
Total Enrollment200
FDA Designations
No designations recorded
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT07215559A Study of Macupatide (LY3532226) and Eloralintide (LY3841136), Alone or in Combination, in Adults With Obesity or Overweight and With Type 2 DiabetesPHASE2 RECRUITING 200Oct 16, 2025May 1, 2027Jun 4, 202642 United States, Argentina +2
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Study Endpoints
Primary Endpoints
Percent Change from Baseline in Body Weight
Baseline, Week 32
Secondary Endpoints
Change from Baseline in Hemoglobin A1c (HbA1c)
Baseline, Week 32
Change from Baseline in Body Mass Index (BMI)
Baseline, Week 32
Change from Baseline in Fasting Glucose
Baseline, Week 32
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Study Design & Arms
AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeTREATMENT
Treatment Arms
ArmTypeDescription
Macupatide (Macupatide + Eloralintide Placebo)EXPERIMENTALParticipants will be administered macupatide subcutaneously (SC) and eloralintide placebo SC
Eloralintide (Elorlintide + Macupatide Placebo)EXPERIMENTALParticipants will be administered eloralintide SC and macupatide placebo SC
Macupatide + EloralintideEXPERIMENTALParticipants will be administered eloralintide SC and macupatide SC
Placebo (Macupatide Placebo + Elorlintide Placebo)PLACEBO_COMPARATORParticipants will be administered eloralintide placebo SC and macupatide placebo SC
Interventions
NameTypeDescription
MacupatideDRUGAdministered SC
EloralintideDRUGAdministered SC
Macupatide PlaceboDRUGAdministered SC
Eloralintide PlaceboDRUGAdministered SC
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Eligibility Criteria
Age Range18 Years — 75 Years
SexALL
Healthy VolunteersNo
Study Sites42

Inclusion Criteria: * Have type 2 diabetes * Have an HbA1c ≥7.5% to ≤10.5% at screening * Have been treated with any of the following, alone or in combination, for at least 3 months prior to screening * Diet and exercise * Stable dose of metformin * Sodium-glucose cotransporter-2 (SGLT2) inh...

Countries:United StatesArgentinaAustraliaPuerto Rico
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Recent Changes (Last 90 Days)
LOWJun 4, 2026NCT07215559lastUpdatePostDate: changed
LOWJun 4, 2026NCT07215559lastUpdatePostDate: changed
LOWJun 4, 2026NCT07215559lastUpdatePostDate: changed
LOWJun 4, 2026NCT07215559lastUpdatePostDate: changed
LOWMay 26, 2026NCT07215559primaryCompletionDate: changed
LOWMay 24, 2026NCT07215559studyFirstPostDate: changed